Alleima Dettingen GmbH
DE-MF-000006113 · Germany · Dettingen/Erms
Alleima Dettingen GmbH is registered in the European database on medical devices as a manufacturer, with 91 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIb | 22 |
|---|---|
| Class IIa | 69 |
Among these devices, 91 are declared sterile, 22 active.
Devices declared under this manufacturer
- 1xSnare Asym.50/NiTi0,62/Litze0,39x2037
- Flat Adenoma Resection Instrument Typ C Ø 30
- FÜ.025-FP-400-S.-W (SDPVS)
- Fü.025-FPPU-460-\
- Fü.035-FPPU-260-G.-S.\
- Fü.035-FPPU-450-G.-S.-J.PU 85mm (SDPVS)
- Fü.035-FPPU-450-W.-S. PU 85 \
- Fü.035-FPPU-460-G.-S. PU-55 (BEOD)
- Fü.035-FPPU-460-G.-S. “Snap-tip“ (SDPVS)
- Fü.035-FPPU-460.G.-S.Skal W. (SDPVS)
- Fü.035-FPUH-150 soft core Type (SDPVS)
- Fü.035-FPUH-260-J-Hydrophil (SDPVS)
Showing 12 of 91 declared devices.
Catalogue references include 600350, 600359, 600383, 600396, 600407, 600460.
European nomenclature codes declared: G99, G03030199, G0305010201, G99,U0699, U0699, U0601.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 91 |
| Country of registration | Germany |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 91 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.
North American profile: Neither register. Alleima Dettingen GmbH was not found in either the U.S. or the Canadian register.